ClinVar Miner

List of variants in gene ADAMTS2 reported as benign by Illumina Clinical Services Laboratory,Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 17
Download table as spreadsheet
HGVS dbSNP
NM_014244.5(ADAMTS2):c.*1468A>G rs2059776
NM_014244.5(ADAMTS2):c.*1486C>A rs1863918
NM_014244.5(ADAMTS2):c.*1586A>G rs888760
NM_014244.5(ADAMTS2):c.*212A>C rs10479525
NM_014244.5(ADAMTS2):c.*2396C>T rs3797615
NM_014244.5(ADAMTS2):c.*2951G>A rs1044205
NM_014244.5(ADAMTS2):c.*2952T>A rs1044209
NM_014244.5(ADAMTS2):c.*842T>C rs10038484
NM_014244.5(ADAMTS2):c.1194C>T (p.Asp398=) rs2278221
NM_014244.5(ADAMTS2):c.2028C>T (p.Asp676=) rs1972715
NM_014244.5(ADAMTS2):c.2532C>T (p.Asp844=) rs2303644
NM_014244.5(ADAMTS2):c.321T>C (p.Ser107=) rs2271212
NM_014244.5(ADAMTS2):c.3529C>T (p.Pro1177Ser) rs1054480
NM_014244.5(ADAMTS2):c.47_49TGC[9] (p.Leu23dup) rs568040559
NM_014244.5(ADAMTS2):c.534+9G>C rs2271213
NM_014244.5(ADAMTS2):c.733G>A (p.Val245Ile) rs398829
NM_014244.5(ADAMTS2):c.786G>A (p.Ala262=) rs423552

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.